BEUDAMED
    34 results · 23ms · Sources: EU EUDAMED, US FDA

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    Merge Hemo

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 25, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 25, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 25, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    TYRX SURGICAL MESH, MODEL SMPC-0501

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    84E SERIES SINGLE PLY WRAPPER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·March 3, 2026

    FREESTYLE LITE

    FDA Adverse Event
    Injury ·Product code NBW·July 7, 2011

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Malfunction ·MEDTRONIC CRYOCATH LP·Product code OAE·June 8, 2013

    GE OEC 6600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 10, 2008

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·October 7, 2025